A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077861



Internal ID21450464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118634541..118634541hg38UCSC Ensembl
chr12:119072346..119072346hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655189
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077861
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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